510(k) K162424 ยท HRS Plate, Fixation, Bone
Ulna Plating System
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Oct 12, 2016 |
| Received | Aug 30, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162424
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.